Editor-in-Chief: Prof Idowu, Olufemi E. Neurological surgery Division, Department of Surgery, LASUCOM/LASUTH, Ikeja, Lagos, Nigeria.
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CLINICAL VIGNETTE2017; 3:2
SURGICAL SITES
INFECTION
SURGICAL SITES
INFECTION
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DR OLAGUNJU, TUNDE AJANIDepartment of Surgery,
Lagos State University Teaching Hospital, IKeja, Lagos, Nigeria
HISTORICAL PERSPECTIVE
Galen (130-200 CE)- was the first to opined that pus from wounds inflicted by the gladiators heralded healing
Koch (Professor of Hygiene and Microbiology,1843-1910)- first recognized the cause of infective foci as secondary to microbial growth in his 19th century postulates
Semmelweis (1818-1865) demonstrated a fivefold reduction in puerperal sepsis by hand washing
Louis Pasteur (French bacteriologist, 1822-1895)- revolutionized the entire concept of wound infection. Lister recognized that antisepsis could prevent infection
Joseph Lister (Professor of Surgery, London, 1827-1912)- used Carbolic acid (phenol) during operations to maintain aseptic conditions
Alexander Fleming (microbiologist, London, 1881-1955) credited with the discovery of penicillin
Halsted (Professor of Surgery, Johns Hopkins University, 1852-1922)- introduced use of rubber gloves
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INTRODUCTION AND EPIDEMIOLOGYSurgical site infections (SSI) are a
type of surgical infection thathas always been a majorcomplication of surgery andtrauma and has beendocumented for 4000-5000years
DEFINITIONSSIs are infections of the tissues, organs, or spaces exposed by surgeons during performance of an invasive procedure occurring within 30 days or 1 year if an implant is present
Account for 14-16% of the estimated 2 million nosocomial infections affecting hospitalized patients in the United States
World Health Organization survey demonstrated a prevalence of nosocomial infections in the range of 3-21%, with wound infections accounting for 5-34% of the total
2002 survey report by the Nosocomial Infection National Surveillance Service (NINSS), indicates that the incidence of hospital acquired infection related to surgical wounds in the United Kingdom is as high as 10% and costs the country's National Health Service approximately 1 billion pounds annually
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CLASSIFICATION
CDC classification
1. Incisional SSIs: can be superficial or deep
2. Organ/space SSIs: affect the rest of the body other than the body wall layers
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SUPERFICIAL INCISIONAL SSI Involves only the skin or subcutaneous tissueIncludes at least one of the followingpurulent drainage is present (culture documentation not required)organisms are isolated from fluid/tissue of the superficial incisionat least one sign of inflammation (eg, pain or tenderness,
induration, erythema, local warmth of the wound) is presentwound is deliberately opened by the surgeonsurgeon or clinician declares the wound infectedwound is not considered a superficial incisional SSI if a stitch
abscess is present; if the infection is at an episiotomy, a circumcision site, or a burn wound; or if the SSI extends into fascia or muscle
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DEEP INCISIONAL SSI
Involves deep soft tissues (eg, fascia and/or muscle) of the incision
Includes at least one of the following
purulent drainage is present from the deep incision but without organ/space involvement
fascial dehiscence or fascia is deliberately separated by the surgeon because of signs of inflammation
a deep abscess is identified by direct examination or during reoperation, by histopathology, or by radiologic examination;
the surgeon or clinician declares that a deep incisional infection is present
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ORGAN SSI
Occurs within 30 days of the operation or within 1 year if an implant is present
Involves anatomic structures not opened or manipulated during the operation
Includes at least one of the following:
purulent drainage is present from a drain placed by a stab wound into the organ/space
organisms are isolated from the organ/space by aseptic culturing technique
an abscess in the organ/space is identified by direct examination, during reoperation, or by histopathologic or radiologic examination
a diagnosis of organ/space SSI is made by the surgeon or clinician
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RISK FACTORSPATIENT FACTORS
Older age
Immunosuppression
Obesity
Diabetes mellitus
Chronic inflammatory process
Malnutrition
Smoking
Renal failure
Peripheral vascular disease
Anemia
Radiation
Chronic skin disease
Carrier state (e.g., chronic Staphylococcus carriage)
Recent operation
LOCAL FACTORS
Open compared to laparoscopic surgery
Poor skin preparation
Contamination of instruments
Inadequate antibiotic prophylaxis
Prolonged procedure
Local tissue necrosis
Blood transfusion
Hypoxia, hypothermia
MICROBIAL FACTORS
Prolonged hospitalization
Toxin secretion
Resistance to clearance (e.g., capsule formation)
Dose of Bacterial inoculum
Virulence of the organism
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CLASSES OF SURGICAL WOUNDS
Classification based on the presumed magnitude of the bacterial load at the time of surgery
Clean wounds (class I) 1-2%: include those in which no infection is present; only skin micro flora potentially contaminate the wound, and no hollow viscus that contains microbes is entered.
*Class I D wounds: are similar except that a prosthetic device(e.g., mesh or valve) is inserted
Clean contaminated wound (class II) <10%: include those in which a hollow viscus such as the respiratory, alimentary, or genitourinary tracts with indigenous bacterial flora is opened under controlled circumstances without significant spillage of contents
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CLASSES OF SURGICAL WOUNDS
Contaminated wounds (class III) 15-20%: Include open accidental wounds encountered early after injury, those with extensive introduction of bacteria into a normally sterile area of the body due to major breaks in sterile technique (e.g., open cardiac massage), gross spillage of viscus contents such as from the intestine, or incision through inflamed, albeit nonpurulent tissue
Dirty wounds (class IV) <40%: Include traumatic wounds in which a significant delay in treatment has occurred and in which necrotic tissue is present, those created in the presence of overt infection as evidenced by the presence of purulent material, and those created to access a perforated viscus accompanied by a high degree of contamination
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MAJOR FINDING ADDITIONAL FINDINGS GRADENormal healing 0
Normal healing with mild bruising or erythema
I
some bruising Iaconsiderable bruising Ib
mild erythema IcErythema plus other signs of
inflammationII
at 1 point IIaaround sutures IIb
along wound IIcaround wound IId
Clear or hemoserous discharge IIIat 1 point only; <= 2 cm IIIa
along wound; > 2 cm IIIblarge volume IIIc
prolonged drainage (> 3 days) IIIdPus IV
at 1 point only; <= 2 cm IVaalong wound; > 2 cm IVb
Deep or severe wound infection with or without tissue breakdown or hematoma requiring aspiration
V
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ASEPSIS WOUND SCORE
SOUTHAMPTON GRADING SCHEME FOR SURGICAL WOUNDS
WORK UP
Laboratory Studies
Gram stain for infective organisms and Staining for fungal elements
Tests for antigens from the organism through enzyme-linked immunoassay (ELISA) or radioimmunoassay
Detection of antibody response to the organism in the host sera.
Detection of RNA or DNA sequences or protein from the infective organism by Northern, Southern, or Western blotting, respectively
Polymerase chain reaction (PCR) to detect small amounts of microbial DNA
ultrasonography
Ultrasonography can be applied to the infected wound area to assess whether there is a collection for which drainage is required
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TREATMENTMainstay of treatment is source control or draining of the infected area.
For a superficial SSI this involves opening the wound at the skin and subcutaneous levels and cleansing the wound, along with dressing changes twice or three times a day
Occasionally, sharp debridement to allow healing of the open wound is necessary. wound-suctioning devices can also be used to minimize the discomfort from more frequent dressing changes and possibly to accelerate wound healing.
Organ SSI - source control can generally be achieved with percutaneous drainage. when it involves a more diffuse area of a human cavity (i.e., diffuse peritonitis, mediastinitis), surgical drainage is encouraged and would include repair of any anatomic cause of infection if present
The use of antibiotics is not the standard for treatment of incisional SSI. They are recommended only as adjunctive therapy when surrounding cellulitis occurs or when treating a deep SSI
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COMPLICATIONS
SIRShyperthermia (> 38°C) or hypothermia (< 36°C)tachycardia (> 90 min–1, no β-blockers) or tachypnea(> 20 min–1)white cell count > 12x109 /L or < 4 x109 /L Sepsis: SIRS with a documented infectionSevere sepsis- sepsis with evidence of one or more organ dysfunction;
respiratory (acute respiratory distress syndrome), cardiovascular (septic shock), renal (acute tubular necrosis), hepatic, blood coagulation systems or central nervous system. Septic manifestations and multiple organ dysfunction syndrome (MODS) are mediated by the release of cytokines such as the interleukins
Septic shock- sepsis plus either hypotension (refractory to intravenous fluids) or hyperlactatemia
MODS may progress into multiple system organ failure (MSOF). In this state, the body’s resistance to infection is reduced
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PREVENTION
MICROORGANISM LOCAL PATIENT
PREOPERATIVE Shorten preoperative stay
Antiseptic shower
preoperatively
Appropriate preoperative hair
removal or no hair removal
Avoid or treat remote site
infections
Antimicrobial prophylaxis
Appropriate preoperative hair removal or no hair removal
• Optimize nutrition • Preoperative
warming • Tight glucose
control (insulin drip)
• Stop smoking
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PREVENTION
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Prevention- Intra-operative agentsNAME PRESENTATION USES COMMENTSChlorhexidine
(Hibiscrub)
Alcoholic 0.5%
Aqueous 4%
Skin preparation; Surgical scrub
in dilute solutions in open wounds
Has cumulative effect. Effective against
Gram-positive organisms, vegetative bacteria,
mycobacteria, moderately active against fungi and
viruses, spore germination is also inhibited and relatively
stable in the presence of pus and body fluids
Cetrimide
(Savlon)
Aqueous Skin preparation; Hand-washing
Instrument and surface cleaning
Good detergent action (quaternary ammonium
compoundssurface-active agent). Ineffective against
bacterial spores, tubercle bacilli, fungi, viruses and many
gram-negative bacteria (Pseudomonas spp. may grow in
stored contaminated solutions)
Povidone–iodine
(Betadine)
Alcoholic 10%
Aqueous 7.5%
Skin preparation; Surgical scrub in
dilute solutions in open wounds
Safe, fast-acting, broad spectrum. Some
sporicidal activity. Anti-fungal
Iodine is not free but combined with
polyvinylpyrrolidone (povidone)
Alcohols 70% ethyl, isopropyl Skin preparation Should be reserved for use as disinfectants
Hypochlorites Aqueous preparations
(Eusol, Milton, Chloramine T)
Instrument and surface cleaning
(debriding agent in open wounds?)
Toxic to tissues
Hexachlorophane Aqueous bisphenol Skin preparation Hand-washing Has action against Gram-negative organisms
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CDC GUIDELINE FOR PREVENTION OF SSI Advise patients to have a full-body shower or
bath with soap (antimicrobial only as needed) or an antiseptic agent no earlier than the night before the day of surgery.
Before cesarean delivery, administer antimicrobial prophylaxis before incision.
In most cases, use an alcohol-based agent for skin preparation in the operating room.
It is not necessary to use plastic adhesive drapes with or without antimicrobial properties to prevent SSIs.
For clean and clean-contaminated procedures, do not give additional prophylactic antimicrobial doses after closing the surgical incision, even if the patient has a drain in place.
Do not apply topical antimicrobial agents to the incision
Maintain intraoperative glycaemic control in diabetic and non diabetic patients, targeting blood glucose levels of less than 200 mg/dL.
Maintain patient normothermia.
In patients with normal lung function undergoing general anaesthesia with endotracheal intubation, administer a higher fraction of inspired oxygen (FIO2) during surgery and after extubation in the immediate postoperative period.
Do not withhold transfused blood products as a means to prevent SSIs.
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REFERENCES
1. Williams NS, Bulstrode CJK, O'Connell PR. Bailey and Love’s short practice of surgery 25th edition. Taylor and Francis. 2008.
2. Townsend CM, Beauchamp RD, Evers BM, Mattox KL. Sabiston textbook of surgery: The Biological Basis of Brunicardi FC, Andersen DK, BilliaModern Surgical Practice, 18th edition. Philadelphia: WB Saunders, 2007.
3. Brunicardi FC, Andersen DK, Billiar TR, Dunn DL, Hunter JG. Schwartz’s principles of surgery 10th edition. McGraw-Hill Professional Publishing. 2014.
4. Hemant Singhal. Surgical Wound Infection Clinical Presentation. Medscape. May 2017.
5. Centers for Disease Control and Prevention Guidelines for the Prevention of Surgical Site Infection, 2017.
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